Gene entry
ITGA9
integrin subunit alpha 9
- Chromosome
- 3
- Cytoband
- 3p22.2
- Variants (rsID)
- 92
ITGA9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p22.2). Its official name is “integrin subunit alpha 9”. The reference table lists 92 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs2507941Benignsingle nucleotide variant
- rs267561Benignsingle nucleotide variant
- rs76424398Benignsingle nucleotide variant
Other listed variants
- rs169111
- rs189897
- rs197730
- rs197770
- rs199279
- rs267526
- rs267567
- rs391224
- rs445938
- rs730173
- rs743395
- rs762308
- rs1155742
- rs1892802
- rs1984311
- rs2019749
- rs2070481
- rs2154762
- rs2162683
- rs2212036
- rs2364663
- rs2507948
- rs2555239
- rs2685112
- rs2844359
- rs2844377
- rs2844394
- rs4678985
- rs6419833
- rs6550491
- rs6550497
- rs6770747
- rs6780883
- rs6782856
- rs6785634
- rs6808722
- rs7642079
- rs9823993
- rs9825420
- rs9871277
- rs11709385
- rs11916374
- rs13065705
- rs13079586
- rs13083457
- rs13087290
- rs13097652
- rs17827605
- rs17828523
- rs34308428
- rs34585805
- rs35669742
- rs57547208
- rs61751189
- rs61762997
- rs62239550
- rs62241494
- rs72862213
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
